Canonical Allele Identifier: CA2574913652
Gene: PHOX2A HGNC NCBI

Linked Data

gnomAD v4: 11-72243710-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72243710A>G , CM000673.2:g.72243710A>G GRCh38
NC_000011.9:g.71954754A>G , CM000673.1:g.71954754A>G GRCh37
NC_000011.8:g.71632402A>G NCBI36
NG_008169.1:g.5467T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298231.5:c.217+78T>C MANE Select ENSP00000298231.5:n.217+78T>C
ENST00000544057.1:n.85+1870T>C
NM_005169.3:c.217+78T>C NP_005160.2:n.217+78T>C
NM_005169.4:c.217+78T>C MANE Select NP_005160.2:n.217+78T>C
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